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7
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Ulcerative colitis.溃疡性结肠炎。
Lancet. 2017 Apr 29;389(10080):1756-1770. doi: 10.1016/S0140-6736(16)32126-2. Epub 2016 Dec 1.
2
Crohn's disease.克罗恩病。
Lancet. 2017 Apr 29;389(10080):1741-1755. doi: 10.1016/S0140-6736(16)31711-1. Epub 2016 Dec 1.
3
Effects of concomitant immunomodulators on the pharmacokinetics, efficacy and safety of adalimumab in patients with Crohn's disease or ulcerative colitis who had failed conventional therapy.在传统治疗失败的克罗恩病或溃疡性结肠炎患者中,联合使用免疫调节剂对阿达木单抗的药代动力学、疗效及安全性的影响。
Aliment Pharmacol Ther. 2017 Jan;45(1):50-62. doi: 10.1111/apt.13838. Epub 2016 Nov 7.
4
Crohn's Disease Activity and Concomitant Immunosuppressants Affect the Risk of Serious and Opportunistic Infections in Patients Treated With Adalimumab.克罗恩病活动度及同时使用的免疫抑制剂影响接受阿达木单抗治疗患者发生严重感染和机会性感染的风险。
Am J Gastroenterol. 2016 Dec;111(12):1806-1815. doi: 10.1038/ajg.2016.433. Epub 2016 Sep 27.
5
Adalimumab or infliximab as monotherapy, or in combination with an immunomodulator, in the treatment of Crohn's disease.阿达木单抗或英夫利昔单抗单药治疗,或与免疫调节剂联合治疗,用于治疗克罗恩病。
Aliment Pharmacol Ther. 2016 Nov;44(10):1102-1113. doi: 10.1111/apt.13808. Epub 2016 Sep 26.
6
Predicting the Individual Risk of Acute Severe Colitis at Diagnosis.预测诊断时急性重症结肠炎的个体风险。
J Crohns Colitis. 2017 Mar 1;11(3):335-341. doi: 10.1093/ecco-jcc/jjw159.
7
Adalimumab Monotherapy and a Combination with Azathioprine for Crohn's Disease: A Prospective, Randomized Trial.阿达木单抗单药治疗及与硫唑嘌呤联合治疗克罗恩病:一项前瞻性随机试验
J Crohns Colitis. 2016 Nov;10(11):1259-1266. doi: 10.1093/ecco-jcc/jjw152. Epub 2016 Aug 26.
8
The Selective Use of Combination Therapy in Patients with Inflammatory Bowel Disease Resistant to Anti-TNF: to Whom, How and How Long?
J Crohns Colitis. 2016 Dec;10(12):1451. doi: 10.1093/ecco-jcc/jjw089. Epub 2016 Apr 28.
9
Immunogenicity of infliximab and adalimumab: what is its role in hypersensitivity and modulation of therapeutic efficacy and safety?英夫利昔单抗和阿达木单抗的免疫原性:其在超敏反应以及治疗效果和安全性调节中起什么作用?
Expert Opin Drug Saf. 2016 Jan;15(1):43-52. doi: 10.1517/14740338.2016.1112375. Epub 2015 Nov 11.
10
Effects of Concomitant Immunomodulator Therapy on Efficacy and Safety of Anti-Tumor Necrosis Factor Therapy for Crohn's Disease: A Meta-analysis of Placebo-controlled Trials.伴随免疫调节剂治疗对肿瘤坏死因子治疗克罗恩病疗效和安全性的影响:安慰剂对照试验的荟萃分析。
Clin Gastroenterol Hepatol. 2015 Dec;13(13):2233-40.e1-2; quiz e177-8. doi: 10.1016/j.cgh.2015.06.034. Epub 2015 Jun 30.

联合治疗的益处取决于克罗恩病的疾病表型和病程。

The benefit of combination therapy depends on disease phenotype and duration in Crohn's disease.

作者信息

Ananthakrishnan A N, Sakuraba A, Barnes E L, Pekow J, Raffals L, Long M D, Sandler R S

机构信息

Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Inflammatory Bowel Disease Center and Division of Gastroenterology, University of Chicago, Chicago, IL, USA.

出版信息

Aliment Pharmacol Ther. 2017 Jul;46(2):162-168. doi: 10.1111/apt.14125. Epub 2017 May 3.

DOI:10.1111/apt.14125
PMID:28470787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5484085/
Abstract

BACKGROUND

The impact of combination therapy on disease-related morbidity in patients with established Crohn's disease (CD) or ulcerative colitis (UC) remains to be well-defined.

AIM

To examine the effect of combination therapy on disease outcomes in CD and UC.

METHODS

Using a multicenter prospective cohort, we classified CD and UC patients as being on monotherapy with anti-TNF or on combination with an immunomodulator. The primary outcome was a composite of new IBD-related surgery, hospitalisations, penetrating complications, need for corticosteroids or new biological at 1 year. Multivariable regression models adjusted for potential confounders.

RESULTS

We included 707 patients with CD (45% combination therapy) and 164 with UC (38% combination therapy). Combination therapy was not associated with reduction in the composite outcome in either CD (OR: 0.87, 95% CI: 0.63-1.22) or UC (OR: 1.45, 95% CI: 0.63-3.38). However, while no difference was noted in those with nonstricturing, nonpenetrating CD, a significant reduction in the likelihood of the outcome was seen in those with stricturing or penetrating CD (30% vs 39%, OR: 0.58, 95% CI: 0.37-0.90). A stronger effect was also observed in those with disease duration <5 years (OR: 0.35, 95% CI: 0.14-0.87) compared to those with a longer duration (OR: 0.75, 95% CI: 0.45-1.27). A similar reduction in occurrence of composite outcome was noted with infliximab and with other anti-TNF biologics.

CONCLUSION

The benefit of combination immunomodulator-biological therapy is stronger in those with complicated Crohn's disease, particularly early on in their disease course.

摘要

背景

联合治疗对已确诊的克罗恩病(CD)或溃疡性结肠炎(UC)患者疾病相关发病率的影响仍有待明确。

目的

研究联合治疗对CD和UC疾病转归的影响。

方法

采用多中心前瞻性队列研究,我们将CD和UC患者分为接受抗TNF单药治疗或联合免疫调节剂治疗。主要结局为1年内新发IBD相关手术、住院、穿透性并发症、使用糖皮质激素或新生物制剂的复合指标。采用多变量回归模型对潜在混杂因素进行校正。

结果

我们纳入了707例CD患者(45%接受联合治疗)和164例UC患者(38%接受联合治疗)。联合治疗与CD(比值比:0.87,95%置信区间:0.63 - 1.22)或UC(比值比:1.45,95%置信区间:0.63 - 3.38)的复合结局降低无关。然而,在非狭窄、非穿透性CD患者中未观察到差异,而在狭窄或穿透性CD患者中结局发生的可能性显著降低(30%对39%,比值比:0.58,95%置信区间:0.37 - 0.90)。与病程较长者(比值比:0.75,95%置信区间:0.45 - 1.27)相比,病程<5年者也观察到更强的效应(比值比:0.35,95%置信区间:0.14 - 0.87)。英夫利昔单抗和其他抗TNF生物制剂在复合结局发生率方面有类似降低。

结论

免疫调节剂 - 生物制剂联合治疗对复杂克罗恩病患者益处更大,尤其是在疾病病程早期。